Product NDC: | 0268-0173 |
Proprietary Name: | CENTER-AL - LOLIUM PERENNE POLLEN |
Non Proprietary Name: | Allergenic Extracts Alum Precipitated |
Active Ingredient(s): | 20000 [PNU]/mL & nbsp; Allergenic Extracts Alum Precipitated |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0268-0173 |
Labeler Name: | ALK-Abello, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103753 |
Marketing Category: | BLA |
Start Marketing Date: | 19750115 |
Package NDC: | 0268-0173-10 |
Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (0268-0173-10) |
NDC Code | 0268-0173-10 |
Proprietary Name | CENTER-AL - LOLIUM PERENNE POLLEN |
Package Description | 10 mL in 1 VIAL, MULTI-DOSE (0268-0173-10) |
Product NDC | 0268-0173 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Allergenic Extracts Alum Precipitated |
Dosage Form Name | INJECTION, SUSPENSION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 19750115 |
Marketing Category Name | BLA |
Labeler Name | ALK-Abello, Inc. |
Substance Name | LOLIUM PERENNE POLLEN |
Strength Number | 20000 |
Strength Unit | [PNU]/mL |
Pharmaceutical Classes | Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |